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Find the reads which correspond to DP of vcf

Hello,

I have a variant of interest at position chrX:124068651-G-T with a DP value of 319. Here, it is

chrX 124068651 . G T 200.121 . DP=319;VDB=2.88188e-20;SGB=-0.693147;RPBZ=-2.38326;MQBZ=0.636315;BQBZ=1.07463;SCBZ=-0.654487;MQ0F=0.0125392;AC=1;AN=2;DP4=122,0,197,0;MQ=58 GT:PL 0/1:233,0,169

I have the sorted, indexed bam file from which I have called the variant. Now, it is essential for me to know the name of the reads which support the particular variant at this position.

For this I use sam2tsv (http://lindenb.github.io/jvarkit/Sam2Tsv.html) to find the reads which have the alternate allele at the position. An example output is as follows:

> #Read-Name    Flag    MAPQ    CHROM   READ-POS0   READ-BASE   READ-QUAL   REF-POS1    REF-BASE    CIGAR-OP
> LH00587:73:22HGLTLT4:5:1102:26223:9839        0       60      chrX  91 T     9     124068651  G     M

And there are such 18683080 entries. It is not possible to have so many entries because we have performed nested pcr to amplify a mutation and then amplicon sequenced it,and the number of mutations cannot be so high.

How do I get the DP=319 which will allow me to just extract the read names of those 319 reads supporting alt allele as shown in the above vcf entries??

Best

bam variant vcf sam2tsv
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updated by Pierre Lindenbaum Pierre Lindenbaum • written by totoroGirl • totoroGirl

And there are such 18683080 entries. It is not possible to have so many entries because we have performed nest

I wrote this tool, how did you use it please ?

usage could be

samtools view -h in.bam "chrX:124068651-124068651" | java -jar jvarkit.jar sam2tsv -R ref.fa | awk '$8==124068651'

otherwise, you could just run:

samtools view in.bam "chrX:124068651-124068651" | cut -f1
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written by Pierre Lindenbaum Pierre Lindenbaum 
java -jar /mnt/beegfs/sbhattacharya/clone_tracing/bam_file/M1/jvarkit/dist/jvarkit.jar sam2tsv -R GCA_000001405.15_GRCh38_no_alt_analysis_set.fna  --regions reg.bed input_sam2tsv_sorted.bam res.txt

reg.bed looks this way: chrX 124068651 124068651

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written by totoroGirl • totoroGirl

reg.bed looks this way: chrX 124068651 124068651

it cannot work anyway, you should get an error message:

[WARN][BedLineCodec]cannot use empty BED interval where start==end. chrX 124068651 124068651 chrX(tab)124068651(tab)124068651. Skipping.

BED files are half-open intervals.

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written by Pierre Lindenbaum Pierre Lindenbaum

jup you are right sorry the updated bed file looks like this:

chrX 124068649 124068651

I then grep "124068651" res.txt > res_filt.txt

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written by totoroGirl • totoroGirl

please try my samtools command above (fixed a few minutes ago, missing -h)

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written by Pierre Lindenbaum Pierre Lindenbaum

yes! I am running it now

but your second suggestion: samtools view in.bam "chrX:124068651-124068651" | cut -f1 will give me all the reads,right? not the one which have the G to T substitution.

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written by totoroGirl • totoroGirl

Okay so I used the command which you mentioned earlier, since I only want the reads which have a G to T substitution, I parsed the output so that: READ-BASE is T and REF-BASE is G, I still have 17879217 entries

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written by totoroGirl • totoroGirl

1 answer

answer here: https://github.com/lindenb/jvarkit/issues/260

the depth was huge:

$ samtools depth -r 'chrX:124068651-124068651' jeter.bam  | awk -F '\t' '$2==124068651'
chrX    124068651   25534522

and the vcf caller most probably downsampled the reads.

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written by Pierre Lindenbaum Pierre Lindenbaum

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